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Myelopathic Patients Undergoing Severe Pediatric Spinal Deformity Surgery Can Improve Neurologic Function to That of Non-Myelopathic Patients by 1-Year Postoperative

  • Meghan Cerpa
  • , Scott L. Zuckerman
  • , Lawrence G. Lenke
  • , Michael P. Kelly
  • , Burt Yaszay
  • , Peter Newton
  • , Paul Sponseller
  • , Mark Erickson
  • , Sumeet Garg
  • , Joshua Pahys
  • , Amer Samdani
  • , Patrick Cahill
  • , Richard McCarthy
  • , David Bumpass
  • , Daniel Sucato
  • , Oheneba Boachie-Adjei
  • , Suken Shah
  • , Munish Gupta
  • Columbia University
  • Washington University St. Louis
  • Rady Children's Hospital
  • Johns Hopkins University
  • Children’s Hospital Colorado
  • Shriners Hospitals for Children
  • The Children's Hospital of Philadelphia
  • University of Arkansas-Medical School
  • Scottish Rite Hospital for Children
  • FOCOS Orthopedic Hospital

Research output: Contribution to journalArticlepeer-review

1 Scopus citations

Abstract

Study Design: Multi-center, prospective, observational cohort. Objective: To compare myelopathic vs. non-myelopathic ambulatory patients in short- and long-term neurologic function, operative treatment, and patient-reported outcomes. Methods: Pediatric deformity patients from 16 centers were enrolled with the following inclusion criteria: aged 10-21 years-old, a Cobb angle ≥100° in either the coronal or sagittal plane or any sized deformity with a planned 3-column osteotomy, and community ambulators. Patients were dichotomized into 2 groups: myelopathic (abnormal preoperative neurologic exam with signs/symptoms of myelopathy) and non-myelopathic (no clinical signs/symptoms of myelopathy). Results: Of 311 patients with an average age of 14.7 ± 2.8 years, 29 (9.3%) were myelopathic and 282 (90.7%) were non-myelopathic. There was no difference in age (P = 0.18), gender (P = 0.09), and Risser Stage (P = 0.06), while more patients in the non-myelopathic group had previous surgery (16.1% vs. 3.9%; P = 0.03). Mean lower extremity motor score (LEMS) in myelopathic patients increased significantly compared to baseline at every postoperative visit: Baseline: 40.7 ± 9.9; Immediate postop: 46.0 ± 7.1, P = 0.02; 1-year: 48.2 ± 3.7, P < 0.001; 2-year: 48.2 ± 7.7, P < 0.001). The non-myelopathic group had significantly higher LEMS immediately postoperative (P = 0.0007), but by 1-year postoperative, there was no difference in LEMS between groups (non-myelopathic: 49.3 ± 3.6, myelopathic: 48.2 ± 3.7, P = 0.10) and was maintained at 2-years postoperative (non-myelopathic: 49.2 ± 3.3, myelopathic: 48.2 ± 5.7, P = 0.09). Both groups improved significantly in all SRS domains compared to preoperative, with no difference in scores in the domains for pain (P = 0.12), self-image (P = 0.08), and satisfaction (P = 0.83) at latest follow-up. Conclusion: In severe spinal deformity pediatric patients presenting with preoperative myelopathy undergoing spinal reconstructive surgery, myelopathic patients can expect significant improvement in neurologic function postoperatively. At 1-year and 2-year postoperative, neurologic function was no different between groups. While non-myelopathic patients had significantly higher postoperative outcomes in SRS mental-health, function, and total-score, both groups had significantly improved outcomes in every SRS domain compared to preoperative.

Original languageEnglish
Pages (from-to)1384-1393
Number of pages10
JournalGlobal Spine Journal
Volume13
Issue number5
DOIs
StatePublished - Jun 2023

Keywords

  • myelopathy
  • neurologic deficit
  • neurologic function
  • pediatric spine surgery
  • scoliosis
  • severe pediatric spinal deformity

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